PYCARD

GeneName

PYCARD

Summary

PYCARD, also known as ASC or hASC, is a 22 kDa protein that plays a critical role in the assembly of inflammasomes, which are multi-protein complexes involved in the innate immune response. It is primarily expressed in the cytoplasm and is associated with various cellular structures including the mitochondrion, nucleus, and endoplasmic reticulum. PYCARD functions as a pattern recognition receptor, recognising pathogen-associated molecular patterns and facilitating the activation of caspases, leading to the release of pro-inflammatory cytokines. This protein is also involved in apoptotic processes and has been shown to interact with various proteins, including interleukin-6 receptors and myosin I, highlighting its diverse functional roles in immune signalling and inflammation.

Importance

PYCARD is relevant to: - The regulation of the innate immune response, particularly in the context of pathogen detection and inflammatory signalling. - Apoptotic pathways, contributing to the understanding of cell death mechanisms in various diseases. - The assembly and function of inflammasomes, which are implicated in numerous inflammatory disorders and autoimmune diseases. - The modulation of cytokine production, influencing the immune response in conditions such as infections and chronic inflammation.

Top Products

For researchers investigating PYCARD, we recommend two excellent primary antibodies. The first is the well-cited polyclonal antibody, Anti-TMS1/ASC antibody (ab175449), which has garnered 52 citations and is particularly effective for immunocytochemistry (ICC). This product is a trusted choice for those focusing on cellular studies of PYCARD. Additionally, we offer the recombinant antibody, Anti-TMS1/ASC antibody [EPR10403] (ab155970), which has been validated for multiple applications, including Western blotting (WB), ICC, and flow cytometry (FC). With 42 citations, this recombinant antibody provides the batch-to-batch consistency that many researchers seek, making it a versatile option for reliable PYCARD detection. The PYCARD ELISA Kit (ab151700), supported by 30 citations, is an excellent option for researchers looking to accurately measure PYCARD levels in their samples.

Abcam Product Citation Summary

The data indicates that PYCARD is being studied in various contexts related to inflammasome activity and pyroptosis, particularly in human dermal fibroblasts and thyroid cells. Additionally, research involving rodent models highlights its role in sepsis and neuroinflammation, suggesting a significant interest in PYCARD's function in immune responses and neurobiology.

Abcam Product Citation Table

Domain

The CARD domain mediates interaction with CASP1 and NLRC4 (PubMed:11967258, PubMed:14634131).

The pyrin domain mediates homotypic interactions with pyrin domains of proteins such as of NLRP3, PYDC1, PYDC2 and AIM2.

Function

Functions as a key mediator in apoptosis and inflammation (PubMed:11103777, PubMed:12646168, PubMed:15030775, PubMed:17349957, PubMed:17599095, PubMed:19158675, PubMed:19158676, PubMed:19234215, PubMed:19494289, PubMed:21487011, PubMed:24630722, PubMed:25847972, PubMed:30674671, PubMed:34678144, PubMed:36050480). Promotes caspase-mediated apoptosis involving predominantly caspase-8 and also caspase-9 in a probable cell type-specific manner (PubMed:11103777, PubMed:12646168). Involved in activation of the mitochondrial apoptotic pathway, promotes caspase-8-dependent proteolytic maturation of BID independently of FADD in certain cell types and also mediates mitochondrial translocation of BAX and activates BAX-dependent apoptosis coupled to activation of caspase-9, -2 and -3 (PubMed:14730312, PubMed:16964285). Involved in innate immune response by acting as an integral adapter in the assembly of various inflammasomes (NLRP1, NLRP2, NLRP3, NLRP6, AIM2 and probably IFI16) which recruit and activate caspase-1 leading to processing and secretion of pro-inflammatory cytokines (PubMed:15030775, PubMed:16982856, PubMed:17349957, PubMed:17599095, PubMed:19158675, PubMed:19158676, PubMed:19234215, PubMed:21487011, PubMed:23530044, PubMed:24630722, PubMed:25847972, PubMed:29440442, PubMed:30674671, PubMed:33980849, PubMed:34678144, PubMed:34706239). Caspase-1-dependent inflammation leads to macrophage pyroptosis, a form of cell death (PubMed:24630722). The function as activating adapter in different types of inflammasomes is mediated by the pyrin and CARD domains and their homotypic interactions (PubMed:14499617, PubMed:19234215, PubMed:24630722). Clustered PYCARD nucleates the formation of caspase-1 filaments through the interaction of their respective CARD domains, acting as a platform for of caspase-1 polymerization (PubMed:24630722). In the NLRP1 and NLRC4 inflammasomes seems not be required but facilitates the processing of procaspase-1 (PubMed:17349957). In cooperation with NOD2 involved in an inflammasome activated by bacterial muramyl dipeptide leading to caspase-1 activation (PubMed:16964285). May be involved in RIGI-triggered pro-inflammatory responses and inflammasome activation (PubMed:19915568). In collaboration with AIM2 which detects cytosolic double-stranded DNA may also be involved in a caspase-1-independent cell death that involves caspase-8 (PubMed:19158675, PubMed:19158676). In adaptive immunity may be involved in maturation of dendritic cells to stimulate T-cell immunity and in cytoskeletal rearrangements coupled to chemotaxis and antigen uptake may be involved in post-transcriptional regulation of the guanine nucleotide exchange factor DOCK2; the latter function is proposed to involve the nuclear form (PubMed:22732093). Also involved in transcriptional activation of cytokines and chemokines independent of the inflammasome; this function may involve AP-1, NF-kappa-B, MAPK and caspase-8 signaling pathways (PubMed:12486103, PubMed:16585594). For regulation of NF-kappa-B activating and inhibiting functions have been reported (PubMed:12486103). Modulates NF-kappa-B induction at the level of the IKK complex by inhibiting kinase activity of CHUK and IKBK (PubMed:12486103, PubMed:16585594). Proposed to compete with RIPK2 for association with CASP1 thereby down-regulating CASP1-mediated RIPK2-dependent NF-kappa-B activation and activating interleukin-1 beta processing (PubMed:16585594). Modulates host resistance to DNA virus infection, probably by inducing the cleavage of and inactivating CGAS in presence of cytoplasmic double-stranded DNA (PubMed:28314590).

Isoform 2

May have a regulating effect on the function as inflammasome adapter.

Isoform 3

Seems to inhibit inflammasome-mediated maturation of interleukin-1 beta.

Post-translational modifications

Phosphorylated.

'Lys-63'-linked polyubiquitination by TRAF3 is critical for speck formation and inflammasome activation (PubMed:25847972). 'Lys-63'-linked deubiquitinated by USP50; a crucial step for NLRP3-mediated inflammasome activation (PubMed:28094437). 'Lys-63'-linked polyubiquitination by PELI1 is also critical for speck formation and inflammasome activation (PubMed:34706239). Deubiquitinated by USP3 that cleaves 'Lys-48'-linked ubiquitin chains and strengthens its stability by blocking proteasomal degradation (PubMed:36050480).

Tissue Specificity

Widely expressed at low levels. Detected in peripheral blood leukocytes, lung, small intestine, spleen, thymus, colon and at lower levels in placenta, liver and kidney. Very low expression in skeletal muscle, heart and brain. Expressed in lung epithelial cells (at protein level) (PubMed:23229815). Detected in the leukemia cell lines HL-60 and U-937, but not in Jurkat T-cell lymphoma and Daudi Burkitt's lymphoma. Detected in the melanoma cell line WM35, but not in WM793. Not detected in HeLa cervical carcinoma cells and MOLT-4 lymphocytic leukemia cells.

Cellular localization

• Cytoplasm
• Inflammasome
• Endoplasmic reticulum
• Mitochondrion
• Nucleus
• Upstream of caspase activation, a redistribution from the cytoplasm to the aggregates occurs. These appear as hollow, perinuclear spherical, ball-like structures (PubMed:11103777, PubMed:12191486, PubMed:15030775). Upon NLRP3 inflammasome activation redistributes to the perinuclear space localizing to endoplasmic reticulum and mitochondria (PubMed:12191486, PubMed:15030775). Localized primarily to the nucleus in resting monocytes/macrophages and rapidly redistributed to the cytoplasm upon pathogen infection (PubMed:19234215). Localized to large cytoplasmic aggregate appearing as a speck containing AIM2, PYCARD, CASP8 and bacterial DNA after infection with Francisella tularensis (By similarity).
• Golgi apparatus membrane
• (Microbial infection) Upon HRSV infection, the protein is mainly located in lipid rafts in the Golgi membrane.

Alternative names

ASC, CARD5, TMS1, PYCARD, Apoptosis-associated speck-like protein containing a CARD, hASC, Caspase recruitment domain-containing protein 5, PYD and CARD domain-containing protein, Target of methylation-induced silencing 1

Database links

swissprot:Q9ULZ3 entrezGene:29108 omim:606838

Other research areas

• Neuroscience